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A Study on Endothelial Function in Patients with Atrial Fibrillation by Cardiac Rehabilitation Exercise Training

A Study on Endothelial Function in Patients with Atrial Fibrillation by Cardiac Rehabilitation Exercise Training

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007264
Enrollment
91
Registered
2022-05-11
Start date
2018-08-20
Completion date
Unknown
Last updated
2022-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others(Exercise training) : Atrial fibrillation patients were randomized into a one-year continuous aerobic interval training (CT) group, a six-month detraining after six months of aerobic interval tr

Sponsors

Pohang Semyung Christianity Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: From the patient medical records, adults with paroxysmal or persistent AF who were willing to participate in a training program and agreed to sign an informed consent form were included

Exclusion criteria

Exclusion criteria: The exclusion criteria were: engagement in high-intensity endurance training three times per week or more; class III or IV heart failure per the New York Heart Association Classification; history of open-heart surgery; left ventricular ejection fraction (LVEF) =40%; severe refractory hypertension; severe cardiac valve disease; moderate or severe pulmonary disease; mental disorder; and an inability to exercise due to a musculoskeletal disorder.

Design outcomes

Primary

MeasureTime frame
Biomarkers of endothelial dysfunction

Secondary

MeasureTime frame
Exercise capacity, quality of life, lipid status, physical activity level, arterial stiffness, cardiac function, atrial fibrillation-induced cardioversions, and number of hospital admissions.

Countries

Korea, Republic of

Contacts

Public ContactSeongdae Kim

Seoul National University Hospital

wwwwrte@naver.com+82-2-2072-3940

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026